US10934284B2ActiveUtilityA1
Aminoquinazoline compounds having anti-inflammatory, antifungal, antiparasitic, and anticancer activity
Est. expiryFeb 1, 2033(~6.6 yrs left)· nominal 20-yr term from priority
Inventors:David M. SimpsonDennis Bryan ZerbyMing LuReid W. Von BorstelRui LiJulian ReadingStephen D. Wolpe
C07D 471/04C07D 241/44C07D 241/20C07D 239/42C07D 235/08C07D 233/60C07D 215/46C07D 215/44C07D 215/42C07D 215/40C07D 215/38C07D 213/74C07D 213/73A61P 33/02A61K 31/704A61K 31/555A61K 31/505A61K 31/4965A61K 31/475A61K 31/4745A61K 31/472A61K 31/4706A61K 31/4425A61K 31/44A61K 31/4164A61K 31/40A01N 43/60A01N 43/50A01N 43/42A61K 2300/00C07D 209/12A61K 31/4709A61K 31/437A61K 31/4184A01N 43/90A01N 43/54C07D 239/94A61K 31/517A61K 31/498A61P 35/00A61K 31/337C07D 401/12A61P 29/00A61P 31/10Y02A50/30Y02P20/582Y02A50/409Y02A50/411
86
PatentIndex Score
2
Cited by
97
References
7
Claims
Abstract
Amine compounds having activity against inflammation, fungi, unicellular parasitic microorganisms, and cancer are described. The compounds contain a monocyclic, bicyclic, or tricyclic aromatic ring having one, two, or three ring nitrogen atoms.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1. A compound represented by Formula IB1 or a pharmaceutically acceptable salt thereof
wherein n is 1;
Q is absent;
R 1 is hydrogen or halo; and
R 7 is phenyl substituted by alkoxy having from 6 to 10 carbon atoms or phenoxy.
2. The compound or salt of claim 1 , wherein the compound is selected from the group consisting of:
N-[3-(Hexyloxy)benzyl]quinazolin-4-amine,
N-[3-(Decyloxy)benzyl]quinazolin-4-amine,
N-[4-(Decyloxy)benzyl]quinazolin-4-amine,
N-[4-(Hexyloxy)benzyl]quinazolin-4-amine.
3. A pharmaceutical composition comprising an effective amount of the compound or pharmaceutically acceptable salt of claim 1 and a pharmaceutically acceptable carrier.
4. The compound or salt of claim 1 , wherein the compound is N-(3-Phenoxybenzyl)quinazolin-4-amine.
5. A pharmaceutical composition comprising an effective amount of the compound or pharmaceutically acceptable salt of claim 4 and a pharmaceutically acceptable carrier.
6. A method of inhibiting a fungus ex vivo, comprising contacting a surface or the fungus with the compound or pharmaceutically acceptable salt of claim 1 .
7. A method of inhibiting a fungus ex vivo, comprising contacting a surface or the fungus with the compound or pharmaceutically acceptable salt of claim 4 .Cited by (0)
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